Wang Qiang, Wang Zuo-Feng, Cao Mei, Wang Zhi-Ying
Department of Pediatrics, Sichuan Province People's Hospital, Sichuan Province, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013 Apr;21(2):469-73. doi: 10.7534/j.issn.1009-2137.2013.02.044.
The aim of this study was to investigate the effects of TLR2, TLR9, CD4(+)CD25(+) regulatory T cells (Treg) and transcription factor FoxP3 in the pathogenesis of children with infectious mononucleosis (IM). Thirty-five acute IM patients admitted in our hospital from April 2010 to January 2011 were enrolled in this study. Thirty-five healthy subjects were taken as control. The thirty-five patients before treatment were considered as patients in acute stage, after treatment and without clinical symptom they were thought as patients in recovery stage. The expression levels of TLR2, TLR9 and FoxP3 mRNA were detected by real time PCR using SYBR Green I. The expression of T lymphocyte subset CD4(+)CD25(+) in peripheral blood mononuclear cells was detected by flow cytometry. The results showed that the relative levels of TLR2 mRNA (4.03 ± 0.56), TLR9 mRNA (8.88 ± 1.56) in peripheral blood mononuclear cells of IM patients in acute stage were significantly higher than those of the controls [TLR2 mRNA (2.22 ± 0.57), TLR9 mRNA (3.63 ± 1.30)] and IM patients in recovery stage [TLR2 mRNA (2.76 ± 0.83), TLR9 mRNA (5.34 ± 1.60)] (P < 0.01). The result of CD4(+)CD25(+) (2.38 ± 1.32%) and relative level of FoxP3 mRNA(2.82 ± 0.90) in peripheral blood mononuclear cells of IM patients in acute stage were lower than those of the control [CD4(+)CD25(+) (7.85 ± 1.97%), FoxP3 mRNA (4.65 ± 1.23) ] (P < 0.01). There was no significant difference in CD4(+)CD25(+) (6.81 ± 1.84%), FoxP3 mRNA(4.11 ± 1.37) levels between IM patients in recovery stage and the controls (P > 0.05). It is concluded that the expression of CD4(+)CD25(+)regulatory T cells is reduced, and its special transcription factor FoxP3 mRNA is down-regulated, but expression levels of TLR2 mRNA, TLR9 mRNA are up-regulated in IM patients of acute stage.
本研究旨在探讨Toll样受体2(TLR2)、Toll样受体9(TLR9)、CD4(+)CD25(+)调节性T细胞(Treg)及转录因子叉头框蛋白3(FoxP3)在传染性单核细胞增多症(IM)患儿发病机制中的作用。选取2010年4月至2011年1月我院收治的35例急性IM患儿作为研究对象,另选35例健康儿童作为对照。将35例患儿治疗前视为急性期患者,治疗后无临床症状者视为恢复期患者。采用SYBR Green I实时荧光定量PCR法检测外周血单个核细胞中TLR2、TLR9及FoxP3 mRNA的表达水平;采用流式细胞术检测外周血单个核细胞中T淋巴细胞亚群CD4(+)CD25(+)的表达。结果显示,急性期IM患儿外周血单个核细胞中TLR2 mRNA相对水平(4.03±0.56)、TLR9 mRNA相对水平(8.88±1.56)显著高于对照组[TLR2 mRNA(2.22±0.57)、TLR9 mRNA(3.63±1.30)]及恢复期IM患儿[TLR2 mRNA(2.76±0.83)、TLR9 mRNA(5.34±1.60)](P<0.01)。急性期IM患儿外周血单个核细胞中CD4(+)CD25(+)表达率(2.38±1.32%)及FoxP3 mRNA相对水平(2.82±0.90)低于对照组[CD4(+)CD25(+)(7.85±1.97%)、FoxP3 mRNA(4.65±1.23)](P<0.01)。恢复期IM患儿外周血单个核细胞中CD4(+)CD25(+)表达率(6.81±1.84%)及FoxP3 mRNA水平(4.11±1.37)与对照组比较,差异无统计学意义(P>0.05)。结论:急性期IM患儿CD4(+)CD25(+)调节性T细胞表达降低,其特异性转录因子FoxP3 mRNA下调,而TLR2 mRNA、TLR9 mRNA表达上调。